A Phase 1/2 interventional study of AdCLD-CoV19 in COVID-19, sponsored by Cellid Co., Ltd.. Completed at 5 sites in Korea, Republic of. Open to participants aged 19 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-07-28.
Sponsored by Cellid Co., Ltd. · Phase 1/2, Interventional, and Prevention
This is a Phase 1/2a clinical trial to assess the safety and immunogenicity of AdCLD-CoV19 in healthy adults.
Part A is conducted as dose-escalation, single-center, open-label, a Phase 1 clinical trial. Part B is conducted as multi-center, open-label, a Phase 2a clinical trial. In Part A, we assess safety in all dose groups and set suitable two doses for Part B. In Part B, we assess immune responses against SARS-CoV-2 and set suitable dose for next phase of clinical trial. DSMB will evaluate safety during the whole study period.
7,638 studies on the registry are indexed under COVID-19; 488 are open to participants now.
This study's enrollment of 150 is above the median of 100 across 4,098 interventional studies indexed under COVID-19.
Browse COVID-19 studies →Cellid Co., Ltd. is the lead sponsor of 8 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Subject will receive single dose of AdCLD-CoV19(2.5x10\^10VP) as intramuscular injection.
Biological: AdCLD-CoV19
Subject will receive single dose of AdCLD-CoV19(5.0x10\^10VP) as intramuscular injection.
Biological: AdCLD-CoV19
Subject will receive single dose of AdCLD-CoV19(1.0x10\^11VP) as intramuscular injection.
Biological: AdCLD-CoV19
Subject will receive single dose of AdCLD-CoV19 as intramuscular injection.
Biological: AdCLD-CoV19
Subject will receive single dose of AdCLD-CoV19 as intramuscular injection.
Biological: AdCLD-CoV19
Replication-defective human adenovirus type 5/35 vector based vaccine expressing S protein of SARS-CoV-2.
Incidence of solicited adverse events(AEs)
Time frame: Through 7 days post-vaccination
Incidence of unsolicited AEs
Time frame: Through 28, 56 days post-vaccination
Incidence of serious adverse events(SAEs)
Time frame: Through 12 months post-vaccination
Incidence of adverse events of special interest(AESIs)
Time frame: Through 12 months post-vaccination
Seroconversion rate(SCR) of neutralization antibody using wild type SARS-CoV-2
Time frame: 4, 8 weeks post-vaccination
Geometric mean titer(GMT) of neutralization antibody using wild type SARS-CoV-2
Time frame: 4, 8 weeks post-vaccination
GMT of S protein specific antibody
Time frame: 2, 4, 8, 26, 52 weeks post-vaccination
Index of T cell response
Time frame: 2, 4, 26, 52 weeks post-vaccination
SCR of neutralization antibody using pseudovirus
Time frame: 2, 4, 8, 26, 52 weeks post-vaccination
GMT of neutralization antibody using pseudovirus
Time frame: 2, 4, 8, 26, 52 weeks post-vaccination
GMT of S protein receptor binding domain(RBD) specific antibody
Time frame: 2, 4, 8, 26, 52 weeks post-vaccination
This study is completed, as verified in Jul 2023. You cannot join it, but the record below documents what was studied.
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Cellid Co., Ltd.